Protective effect of probiotics in rats with acute-on-chronic liver failure and related mechanism

ObjectiveTo investigate the effect of probiotics intervention on rats with acute-on-chronic liver failure (ACLF) and related mechanism. MethodsA total of 44 male Sprague-Dawley rats were randomly divided into six groups using a random number table, i.e., control group 1 (C1 group with 6 rats without...

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Main Author: ZHANG Yongchao
Format: Article
Language:zho
Published: Editorial Department of Journal of Clinical Hepatology 2019-07-01
Series:Linchuang Gandanbing Zazhi
Online Access:http://www.lcgdbzz.org/qk_content.asp?id=10027
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spelling doaj-6872100841eb43fd8dd2cc1e111dc61a2020-11-25T00:11:59ZzhoEditorial Department of Journal of Clinical HepatologyLinchuang Gandanbing Zazhi1001-52561001-52562019-07-0135715701575Protective effect of probiotics in rats with acute-on-chronic liver failure and related mechanismZHANG Yongchao0School of Clinical Medicine, Jining Medical College, Jining, Shandong 272000, ChinaObjectiveTo investigate the effect of probiotics intervention on rats with acute-on-chronic liver failure (ACLF) and related mechanism. MethodsA total of 44 male Sprague-Dawley rats were randomly divided into six groups using a random number table, i.e., control group 1 (C1 group with 6 rats without any intervention), model group 1 (M1 group with 8 rats treated with intraperitoneally injected 40% CCl4 oil solution for 10 weeks, followed by phosphate-buffered saline by gavage since week 7 and D-galactosamine acute attack at the end of week 10), probiotics intervention group 1 (Y1 group with 8 rats treated with the same modeling method as the M1 group, and probiotics solution was given by gavage), control group 2 (C2 group with 6 rats without any intervention), model group 2 (M2 group with 8 rats treated with intraperitoneally injected 40% CCl4 oil solution, followed by D-galactosamine acute attack at the end of week 10 and phosphate-buffered saline by gavage at 48 hours after attack, and they were sacrificed at the end of week 12), and probiotics intervention group 2 (Y2 group with 8 rats treated with the same modeling method as the M2 group, and probiotics solution was given by gavage). Body weight, liver function, and liver histopathology were observed before and after intervention. ELISA was used to measure the levels of endotoxin and endocrine immunoglobulin A (sIgA) in plasma, Western Blot was used to measure the content of the intestinal tight junction protein Occludin, RT-PCR was used to measure the mRNA expression of Occludin and ZO-1, and a selective medium was used to measure the changes in related indices including intestinal flora. A one-way analysis of variance was used for comparison of continuous data between multiple groups, and the SNK-q test was used for further comparison between two groups. ResultsThere were significant differences in body weight, liver index, alanine aminotransferase, aspartate aminotransferase, total bilirubin, plasma endotoxin, sIgA, and mRNA expression of Occludin and ZO-1 between the C1, M1, and Y1 groups (F=27.65, 8.96, 61.37, 18.27, 21.00, 87.01, 67.10, 101.50, and 10540, all P<0.05), as well as between the C2, M2, and Y2 groups (F=14.04, 12.85, 14.02, 11.39, 35.80, 19.14, 15.37, 2502, and 126.00, all P<0.05). There was no significant difference in the protein expression of Occludin between the C1, M1, and Y1 groups (F=16.40, P<0.05). There were significant differences in the content of Lactobacillus, Bifidobacterium, Enterococcus, and Enterobacter between the C1, M1, and Y1 groups (F=77.95, 66.61, 25.63, and 33.29, all P<0.05), as well as between the C2, M2, and Y2 groups (F=21.50, 22.62, 6.71, and 17.74, all P<0.05). ConclusionIntestinal flora disturbance and intestinal barrier dysfunction are observed in rats with ACLF, and probiotics intervention can remodel the structure of intestinal flora, maintain intestinal barrier function, and promote liver repair.http://www.lcgdbzz.org/qk_content.asp?id=10027
collection DOAJ
language zho
format Article
sources DOAJ
author ZHANG Yongchao
spellingShingle ZHANG Yongchao
Protective effect of probiotics in rats with acute-on-chronic liver failure and related mechanism
Linchuang Gandanbing Zazhi
author_facet ZHANG Yongchao
author_sort ZHANG Yongchao
title Protective effect of probiotics in rats with acute-on-chronic liver failure and related mechanism
title_short Protective effect of probiotics in rats with acute-on-chronic liver failure and related mechanism
title_full Protective effect of probiotics in rats with acute-on-chronic liver failure and related mechanism
title_fullStr Protective effect of probiotics in rats with acute-on-chronic liver failure and related mechanism
title_full_unstemmed Protective effect of probiotics in rats with acute-on-chronic liver failure and related mechanism
title_sort protective effect of probiotics in rats with acute-on-chronic liver failure and related mechanism
publisher Editorial Department of Journal of Clinical Hepatology
series Linchuang Gandanbing Zazhi
issn 1001-5256
1001-5256
publishDate 2019-07-01
description ObjectiveTo investigate the effect of probiotics intervention on rats with acute-on-chronic liver failure (ACLF) and related mechanism. MethodsA total of 44 male Sprague-Dawley rats were randomly divided into six groups using a random number table, i.e., control group 1 (C1 group with 6 rats without any intervention), model group 1 (M1 group with 8 rats treated with intraperitoneally injected 40% CCl4 oil solution for 10 weeks, followed by phosphate-buffered saline by gavage since week 7 and D-galactosamine acute attack at the end of week 10), probiotics intervention group 1 (Y1 group with 8 rats treated with the same modeling method as the M1 group, and probiotics solution was given by gavage), control group 2 (C2 group with 6 rats without any intervention), model group 2 (M2 group with 8 rats treated with intraperitoneally injected 40% CCl4 oil solution, followed by D-galactosamine acute attack at the end of week 10 and phosphate-buffered saline by gavage at 48 hours after attack, and they were sacrificed at the end of week 12), and probiotics intervention group 2 (Y2 group with 8 rats treated with the same modeling method as the M2 group, and probiotics solution was given by gavage). Body weight, liver function, and liver histopathology were observed before and after intervention. ELISA was used to measure the levels of endotoxin and endocrine immunoglobulin A (sIgA) in plasma, Western Blot was used to measure the content of the intestinal tight junction protein Occludin, RT-PCR was used to measure the mRNA expression of Occludin and ZO-1, and a selective medium was used to measure the changes in related indices including intestinal flora. A one-way analysis of variance was used for comparison of continuous data between multiple groups, and the SNK-q test was used for further comparison between two groups. ResultsThere were significant differences in body weight, liver index, alanine aminotransferase, aspartate aminotransferase, total bilirubin, plasma endotoxin, sIgA, and mRNA expression of Occludin and ZO-1 between the C1, M1, and Y1 groups (F=27.65, 8.96, 61.37, 18.27, 21.00, 87.01, 67.10, 101.50, and 10540, all P<0.05), as well as between the C2, M2, and Y2 groups (F=14.04, 12.85, 14.02, 11.39, 35.80, 19.14, 15.37, 2502, and 126.00, all P<0.05). There was no significant difference in the protein expression of Occludin between the C1, M1, and Y1 groups (F=16.40, P<0.05). There were significant differences in the content of Lactobacillus, Bifidobacterium, Enterococcus, and Enterobacter between the C1, M1, and Y1 groups (F=77.95, 66.61, 25.63, and 33.29, all P<0.05), as well as between the C2, M2, and Y2 groups (F=21.50, 22.62, 6.71, and 17.74, all P<0.05). ConclusionIntestinal flora disturbance and intestinal barrier dysfunction are observed in rats with ACLF, and probiotics intervention can remodel the structure of intestinal flora, maintain intestinal barrier function, and promote liver repair.
url http://www.lcgdbzz.org/qk_content.asp?id=10027
work_keys_str_mv AT zhangyongchao protectiveeffectofprobioticsinratswithacuteonchronicliverfailureandrelatedmechanism
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